Apert syndrome is a rare genetic disorder, characterized by premature fusion of skull sutures, mid-face hypoplasia and syndactyly of the hands and feet.It is inherited as autosomal dominant or sporadic and is associated with increased paternal age.It arises from mutations in the fibroblast growth factor receptor 2 gene on chromosome 10q26.A case of
Umbilical discharge in infancy is often attributed to infection or an umbilical granuloma.It is important to investigate if such a discharge is due to an Patio Occasional Table underlying congenital abnormality because corrective surgical intervention may then be required.We present the first case of an infant with a persistent umbilical discharge
This article serves as an introduction to a collection of selected papers presented at the ACNS Conference on Cloud and Immersive Technologies in Ball Education (CITEd 2022), which took place in Kyiv, Ukraine, on December 21-22, 2022.The collection provides valuable insights into the latest advancements in cloud and immersive technologies in the fi
This article serves as an introduction to a collection of selected papers presented at the ACNS Conference on Cloud and Immersive Technologies in Ball Education (CITEd 2022), which took place in Kyiv, Ukraine, on December 21-22, 2022.The collection provides valuable insights into the latest advancements in cloud and immersive technologies in the fi
In modern wargaming, accurately predicting the locations of the opponent units is crucial for effective strategy and decision making.However, situational data provided by tactical wargame systems present significant challenges: high redundancy across consecutive frames and extreme data sparsity, with units occupying only a Patio Occasional Table sm